BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    URISCREEN

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AXSOS

    FDA UDI
    Stryker GmbH·07613154730025·X-Ray Template - Dist. Femur Plate TS

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981084·anteriors; shade A3.5; mould CM6

    PENTAX Video Colonoscopes (EC Family)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COLORISE RIGID

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code DTB·February 19, 2013

    DURATA

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code NVY·December 31, 2010

    IMPULSE GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQO·August 5, 2014

    The Bigger Better-Bladder, Catalog Number BBB38 (with 3/8 inch ID tubing), Sterile, Single use only --- Manufactured for: Circulatory Technology Inc., 21 Singworth Street, Oyster Bay, 11771 (516) 624-2424 --- 510 (k) 981284.

    FDA Recall
    Terminated ·Circulatory Technology Inc·Product code DTN·June 3, 2009